Clinical Research Coordinator III

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine , which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers , which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

To learn more about Care Access, visit www.CareAccess.com .

How This Role Makes a Difference

The Clinical Research Coordinator ’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening , enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance . The CRC III is responsible for the most pivotal and complex protocols and study designs being conducted at Care Access Research sites.

How You'll Make An Impact

Patient Coordination

Manages some of the sites most challenging therapeutic areas and study designs

High complexity; intensive assessments, multi‑arm trials, frequent sponsor interaction.

Champions balancing protocol needs with patient experience and safety across studies; models best practices.

Can operate as solo CRC onsite.

Prescreen study candidates

Obtain informed consent per Care Access SOP

Complete visit procedures in accordance with protocol.

Complete basic clinical procedures per protocol, such as blood draws, vital signs, ECGs, etc.

Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.

Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.

Prioritize activities with specific regard to protocol timelines

Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.

Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.

Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)

Documentation

Record data legibly and enter in real time on paper or e-source documents

Accurately record study medication inventory, medication dispensation, and patient compliance.

Resolve data management queries and correct source data within sponsor provided timelines

Assist regulatory personnel with completion and filing of regulatory documents.

Assist in the creation and review of source documents.

Patient Recruitment

Assist with planning and creation of appropriate recruitment materials.

Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.

Actively work with recruitment team in calling and recruiting subjects

Site Support

Primary point of contact for the site

Supports Key Sponsors and CROs

Responsible for mentoring and training CRAs and CRC I/CRC II to ensure complete understanding of Care Access processes, SOPs, and values, ensuring that they are successful during their transition to more demanding opportunities and responsibilities

Supports training and process improvements.

Assist Regional Site Director, Operational Compliance and Quality Assurance Departments with all Care Quality and FDA audits

Develops and maintains CAPAs, when needed, with approvals from the Regional Site Director

Review and assess protocol (including amendments) for clarity, logistical feasibility

Sets quality standards; prepares for audits; leads corrective actions.

Other Responsibilities:

Leads complex studies; coaches team; influences site operations.

Ensure that all training and study requirements are met prior to trial conduct.

Communicate clearly verbally and in writing.

Attend Investigator meetings as required.

Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)

Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.

Maintain effective relationships with study participants and other care Access Research personnel.

Demonstrate deep knowledge about the therapeutic area of responsibility including comprehensive understanding of related Protocol designs, outcomes and timelines

Drives improvements; removes barriers; mentors others through change.

The Expertise Required

Ability to understand and follow institutional SOPs.

Excellent working knowledge of medical and research terminology

Excellent working knowledge of federal regulations, good clinical practices (GCP)

Ability to communicate and work effectively with a diverse team of professionals.

Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail

Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.

Critical thinker and problem solver

Friendly, outgoing personality; maintain a positive attitude under pressure.

High level of self-motivation and energy

Excellent professional writing and communication skills

Ability to work independently in a fast-paced environment with minimal supervision.

Engage in continuous independent learning within the therapeutic area of responsibility

Leads cross‑site communications; represents site with sponsors/CROs.

Highly autonomous; leads study execution and resolves operational challenges independently

Certifications/Licenses, Education, and Experience

Minimum Education:

Bachelor’s Degree preferred, or equivalent combination of education, training and experience.

Minimum Experience:

A minimum of 5 years prior Clinical Research Coordinator experience required

Prefer 1 year of experience as a Care Access Research Clinical Research Coordinator

Recent phlebotomy experience required

How We Work Together

Location : This is an on-site position with regional commute requirements

Travel : This role requires up to 10% travel requirements further explained below. Length of travel will depend upon study requirements, staff needs, and company initiatives.

Physical demands associated with this position Include : The ability to use keyboards and other computer equipment.

Walking, Standing, Sitting, Lifting (up to and over 25lbs, as well as overhead), Driving ~ 20%

The expected pay range for this role is $65,000 - $95,000 USD per year for full time team members.

Benefits & Perks (US Full Time Employees)

Paid Time Off (PTO) and Company Paid Holidays

100% Employer paid medical, dental, and vision insurance plan options

Health Savings Account and Flexible Spending Accounts

Bi-weekly HSA employer contribution

Company paid Short-Term Disability and Long-Term Disability

401(k) Retirement Plan, with Company Match

Mandatory Employer Disclosures

• Notice to Illinois applicants: Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.
• Notice to Connecticut applicants: Care Access may require applicants to submit to a urin